Colon Cancer: Gene >> SLC2A10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359271
Start	46725759:46725759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723C>A
AA Mutation	p.Phe241Leu(p.F241L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359271
Start	46725241:46725241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.205A>G
AA Mutation	p.Ile69Val(p.I69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359271
Start	46726878:46726878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1303C>T
AA Mutation	p.Leu435Phe(p.L435F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359271
Start	46725923:46725923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558025597
CDS Mutation	c.887G>A
AA Mutation	p.Arg296His(p.R296H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359271
Start	46725458:46725458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.422C>T
AA Mutation	p.Ala141Val(p.A141V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359271
Start	46726189:46726189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1153G>T
AA Mutation	p.Ala385Ser(p.A385S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359271
Start	46725901:46725901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.865G>C
AA Mutation	p.Gly289Arg(p.G289R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359271
Start	46726033:46726033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997C>A
AA Mutation	p.Pro333Thr(p.P333T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359271
Start	46725487:46725487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451T>C
AA Mutation	p.Tyr151His(p.Y151H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359271
Start	46725680:46725680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774497964
CDS Mutation	c.644G>A
AA Mutation	p.Arg215Gln(p.R215Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359271
Start	46725273:46725273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201323237
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359271
Start	46725366:46725366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199848479
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359271
Start	46725867:46725867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142697617
CDS Mutation	c.831C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359271
Start	46725711:46725711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC2A10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359271
Start	46729473:46729473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1532A>G
AA Mutation	p.Gln511Arg(p.Q511R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359271
Start	46725693:46725693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000359271
Start	46726942:46726942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1367G>A
AA Mutation	p.Trp456Ter(p.W456*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript